WO2010014841A1 - Synthèse et formulations de sels de moutarde d'isophosphoramide et de leurs analogues - Google Patents

Synthèse et formulations de sels de moutarde d'isophosphoramide et de leurs analogues Download PDF

Info

Publication number
WO2010014841A1
WO2010014841A1 PCT/US2009/052295 US2009052295W WO2010014841A1 WO 2010014841 A1 WO2010014841 A1 WO 2010014841A1 US 2009052295 W US2009052295 W US 2009052295W WO 2010014841 A1 WO2010014841 A1 WO 2010014841A1
Authority
WO
WIPO (PCT)
Prior art keywords
compound
formula
formulation
nhch
amine
Prior art date
Application number
PCT/US2009/052295
Other languages
English (en)
Other versions
WO2010014841A8 (fr
Inventor
Frank Walter Waligora
John C. Amedio
Original Assignee
Ziopharm Oncology, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to US13/056,628 priority Critical patent/US8664201B2/en
Priority to EP09803607.2A priority patent/EP2318013A4/fr
Priority to NZ590995A priority patent/NZ590995A/xx
Priority to AU2009276512A priority patent/AU2009276512B2/en
Priority to MX2011001122A priority patent/MX2011001122A/es
Priority to EA201170277A priority patent/EA022655B1/ru
Priority to BRPI0916739A priority patent/BRPI0916739A2/pt
Priority to CA2732290A priority patent/CA2732290A1/fr
Application filed by Ziopharm Oncology, Inc. filed Critical Ziopharm Oncology, Inc.
Priority to JP2011521338A priority patent/JP5711660B2/ja
Priority to CN200980133758XA priority patent/CN102137674A/zh
Publication of WO2010014841A1 publication Critical patent/WO2010014841A1/fr
Priority to IL210921A priority patent/IL210921A/en
Priority to ZA2011/00878A priority patent/ZA201100878B/en
Publication of WO2010014841A8 publication Critical patent/WO2010014841A8/fr
Priority to US14/167,169 priority patent/US9145431B2/en
Priority to US14/806,720 priority patent/US9254298B2/en
Priority to US14/987,185 priority patent/US20160215005A1/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/06—Phosphorus compounds without P—C bonds
    • C07F9/22—Amides of acids of phosphorus
    • C07F9/222—Amides of phosphoric acids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/66—Phosphorus compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/66—Phosphorus compounds
    • A61K31/664—Amides of phosphorus acids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/66—Phosphorus compounds
    • A61K31/675—Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/36—Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
    • A61K47/38—Cellulose; Derivatives thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/06—Phosphorus compounds without P—C bonds
    • C07F9/08—Esters of oxyacids of phosphorus
    • C07F9/09—Esters of phosphoric acids
    • C07F9/14—Esters of phosphoric acids containing P(=O)-halide groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/06—Phosphorus compounds without P—C bonds
    • C07F9/08—Esters of oxyacids of phosphorus
    • C07F9/09—Esters of phosphoric acids
    • C07F9/14—Esters of phosphoric acids containing P(=O)-halide groups
    • C07F9/1406—Esters of phosphoric acids containing P(=O)-halide groups containing the structure Hal-P(=O)-O-aryl
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/06—Phosphorus compounds without P—C bonds
    • C07F9/16—Esters of thiophosphoric acids or thiophosphorous acids
    • C07F9/165—Esters of thiophosphoric acids
    • C07F9/20—Esters of thiophosphoric acids containing P-halide groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/06—Phosphorus compounds without P—C bonds
    • C07F9/22—Amides of acids of phosphorus
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/06—Phosphorus compounds without P—C bonds
    • C07F9/22—Amides of acids of phosphorus
    • C07F9/24—Esteramides
    • C07F9/2404—Esteramides the ester moiety containing a substituent or a structure which is considered as characteristic
    • C07F9/2429—Esteramides the ester moiety containing a substituent or a structure which is considered as characteristic of arylalkanols
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/06—Phosphorus compounds without P—C bonds
    • C07F9/22—Amides of acids of phosphorus
    • C07F9/24—Esteramides
    • C07F9/2454—Esteramides the amide moiety containing a substituent or a structure which is considered as characteristic
    • C07F9/2458—Esteramides the amide moiety containing a substituent or a structure which is considered as characteristic of aliphatic amines

Definitions

  • prodrugs such as phosphoramide compounds, which can be activated by the high concentration of phosphoramidases present in neoplastic cells, have been investigated.
  • Two phosphoramide alkylating agents, cyclophosphamide (CPA) and the isomeric compound ifosfamide (IFOS) have demonstrated effectiveness in the treatment of a broad range of solid tumors and hematological cancers (Zhang et al., Current Drug Therapy 1 : 55-84 (2006)).
  • CPA and IFOS are used both as single agents as well as in combination with other anticancer agents to obtain synergistic antitumor effects.
  • CPA can also be used as an immunosuppressant to treat autoimmune diseases such as rheumatoid arthritis and systemic lupus erythematosus (SLE) (Petri et al, Lupus 13:366-371 (2006); Leandro et al. Ann., Rheum. Dis. 61 : 883-888 (2002); Verberg et al, Arthritis Rheum. 52: 421-424 (2005)).
  • SLE systemic lupus erythematosus
  • CPA and IFOS are prodrugs that are activated intracellularly by 4-hydroxylation by the cytochrome (CYP) P450 oxidases, primarily CYP3A4, CYP2C9 and CYP2B6 in the liver, to produce cytotoxic nitrogen mustards that can react with DNA.
  • CYP cytochrome
  • Acrolein is a byproduct of this reaction.
  • CPA and IFOS The in vivo metabolism of CPA and IFOS also involves inactivation by N- decholoroethylation by CYP3A4/5 and CYP2B6 prior to their conversion to the nitrogen mustards, resulting in production of dechloroethylated metabolites and the byproduct chloroacetaldehyde (CAA).
  • Acrolein and CAA are implicated in toxicities of CPA and IFOS that are unrelated to the cytotoxic mechanism of action of the nitrogen mustard molecules (Zhang et al., Current Drug Therapy 1 : 55-84 (2006)). Acrolein causes the urotoxicity, hemorrahagic cystitis, and liver damage, and CAA causes neurotoxicity and has also been implicated in renal toxicity.
  • the nitrogen mustards of CPA and IFOS, phosphoramide mustard and isophosphoramide mustard, are bifunctional alkylating agents that bind covalently to nucleophilic groups of nucleic acids.
  • the mustards are dechlorinated to produce carbonium ions that react covalently with N 7 of guanine residues.
  • the reaction is referred to as DNA alkylation.
  • Both inter- or intra-strand crosslinks result from the ability of each mustard molecule to react with two guanine residues (Zhang et al, Current Drug Therapy 1 : 55-84 (2006)). Because the inter-strand crosslinks prevent strand separation required for DNA replication, DNA-alkylation is considered to be the major mechanism responsible for the inhibition of cell division by CPA and IFOS.
  • the DNA damage In addition to the antiproliferative (cytostatic) effect, the DNA damage also induces apoptosis, i.e., programmed cell death (O'Conner et al, Cancer Res. 1 : 6550- 6557; (1991); Bahtia et al, Clin. Cancer Res. 1 : 873-880 (1995)).
  • the cytotoxic/cytostatic effects of the nitrogen mustards are mainly responsible for the antitumor activity of CPA and IFOS and, by preventing the proliferative expansion of autoreactive lymphocytes, also for the immunosuppressant activity of CPA in autoimmune disease.
  • isophosphoramide mustard interacts with DNA with a higher affinity than phosphoramide mustard (Boal et al, J. Med. Chem. 32: 1768-1773; 1989). Structural differences involving the intramolecular distance between the chloroethyl groups and their orientation appear to be responsible for the different affinities of the two mustards (Springer et al, J. Org. Chem. 63: 7218-7222 (1998)).
  • IPM cytotoxic nitrogen mustards
  • the "off-target" toxicities and the drug resistance associated with the prodrugs may be reduced.
  • IPM has been synthesized and preliminary biological evaluations of the compound have been conducted; but, unfortunately, IPM itself is unstable and difficult to use directly for human treatment. Stabilized formulations of IPM might further reduce toxicity and allow metronomic administration of doses that are sufficient for both direct cytotoxicity against the tumor and antiangiogenic activity. Improved methods for formulation and manufacture of IPM and analogues and salts thereof are needed.
  • IPM salts and analogues of the invention include compounds of formula (E):
  • the invention relates to pharmaceutical formulations comprising a compound of formula (E) and one or more pharmaceutically acceptable carriers. Methods of preparing such compounds and formulations are also described. DETAILED DESCRIPTION
  • IPM salts and analogues of the invention include compounds of formula (E):
  • X and Y independently represent leaving groups such as Cl, Br, I, or a sulfonate, e.g., toluenesulfonate, methanesulfonate, 2,4,6- triisopropylbenzenesulfonate, or 2,4,6-trimethylbenzenesulfonate; and
  • a + is an ammonium cation.
  • Formulations of the invention include IPM salts and analogues together with a lubricant, a diluent and a disintegrant.
  • Formulations of the invention may further comprise additional excipients such as a binder and a compression filler.
  • the disclosure further concerns the synthetic preparation of IPM salts and analogues thereof.
  • the formulations disclosed herein include IPM and IPM analogs that are formulated with one or more equivalents of base.
  • the disclosed compounds are salts of isophosphoramide mustard or isophosphoramide mustard analogs including one or more cations.
  • the cations can be a conjugate acid of an amine base or can be a quaternary ammonium cation.
  • Suitable counterions for isophosphoramide and its analogs include the conjugate acids (as used herein, terms that refer to amines should be understood to include their conjugate acids unless the context indicates that the free amine is intended) of bases including basic amino acids, aliphatic amines, heterocyclic amines, aromatic amines, pyridines, guanidines, and amidines.
  • NHCH 2 CH 2 Y (E); is selected from a primary, secondary or tertiary amine.
  • a of formula (E) represents at least one primary amine such as lysine, arginine, alanine, asparagine, aspartic acid, cysteine, glutamic acid, glutamine, glycine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, serine, threonine, tryptophan, tyrosine, valine, 2-aminoethanol, or tris(hydroxymethyl)aminomethane.
  • a of formula (E) represents at least one secondary amine such as diethylamine, 2- (methylamino)ethanol, aziridine, azetidine, pyrrolidine and piperidine.
  • a of formula (E) represents at least one tertiary amine, such as triethylamine, trimethylamine, N, jV-diisopropylethylamine, and 2- (dimethylamino)ethanol.
  • Primary, secondary, and tertiary amine as used herein refers to the number of direct single bonds between a nitrogen and carbon atom(s), the remainder of the three valencies of the neutral amine being filled by hydrogen atoms.
  • a primary amine has only one direct bond between nitrogen and carbon, while a secondary amine is singly bound to exactly two carbons, a tertiary amine is singly bound to exactly three carbons.
  • Quarternary ammonium cations have four single bonds to carbon atoms, the fourth bond involving the lone pair of the nitrogen atom as well as the three valencies ordinarily present in primary, secondary, and tertiary amines. Accordingly, as the name implies, such species carry a positive charge.
  • a molecule In order for a molecule to be classified within a particular amine type, e.g., primary, secondary or tertiary amine, the molecule must comprise at least one nitrogen with the indicated bonding pattern to carbon(s).
  • a primary amine comprises at least one nitrogen that is singly bound to exactly one carbon atom.
  • a molecule may however comprise more than one type of amine, e.g., 2-aminopiperidine comprises both primary and secondary amine functionality.
  • the amine is an aliphatic amine, such as an acyclic aliphatic amine. In certain embodiments, the amine is an acyclic aliphatic amine, e.g., an amine having 2-3 branched or straight chain alkyl substituents. In certain embodiments, each branched or straight chain alkyl substituent is a C 3 -C 10 alkyl amine, such as a C3-C5 alkyl amine. In certain such embodiments, one or more of the branched or straight chain alkyl substituents are optionally substituted, such as with one or more hydroxyl substituents, e.g., 1, 2, 3 or 4 hydroxyl substituents.
  • Exemplary amines (and their corresponding ammonium ions) for use in the formulations or methods of the invention include pyridine, N, N- dimethylaminopyridine, diazabicyclononane, diazabicycloundecene, N-methyi-N- ethylamine, diethylamine, triethylamine, N, N-diisopropylethylamine, mono-, bis-, or tris-(2-hydroxyethyl)amine, 2-hydroxy-tert-butylamine, tris(hydroxymethyl)methylamine, N, N-dimethyl-N-(2-hydroxyethyl)amine, tri-(2- hydroxyethyl)amine and N-methyl-D-glucamine.
  • the salts described above in formula (E) can include a second amine or ammonium group.
  • the compounds disclosed herein include more than one equivalent of an amine for each equivalent of isophosphoramide mustard or isophosphoramide mustard analog. Such embodiments include those having non-integer ratios of amine to isophosphoramide mustard or isophosphoramide mustard analogs.
  • the compounds have a two to one or three to one ratio of amine to isophosphoramide mustard or an isophosphoramide mustard analog.
  • salts were produced containing two equivalents of amine base per equivalent of isophosphoramide mustard.
  • an amine base used to form isophosphoramide mustard and isophosphoramide mustard analog salts includes more than one amino group; such bases can be termed "multibasic.” More specifically, certain examples of multibasic bases that can be used have two amino groups; such compounds can be referred to as "dibasic.” For example, one suitable dibasic molecule is N 5 N- dimethylaminopyridine, which includes two basic amino groups. In a particular embodiment of a compound disclosed herein, a compound includes isophosphoramide mustard or an isophosphoramide mustard analog and one equivalent of a dibasic amine.
  • the disclosed compounds include one or more zwitterionic bases.
  • bases include basic amino acids, which are zwitterionic at physiological pH.
  • aliphatic amine refers to a compound of the formula NR 1 R 2 R 3 , wherein at least one of R 1 , R 2 or R 3 is an aliphatic group.
  • acyclic aliphatic amine refers to an aliphatic amine as above, wherein at least one, and preferably all, of the aliphatic groups is acyclic.
  • heterocyclic amine refers to a compound of the formula NR 1 R 2 R 3 , wherein at least one of R 1 , R 2 or R 3 is a heterocyclic group or R 1 , R 2 and/or R 3 taken together with their common nitrogen atom form a ring.
  • leaving group refers to a group that can be displaced by a nucleophile.
  • leaving group refers to a group that can be displaced to form an aziridinium intermediate, or can be directly displaced by a biomolecular nucleophile, such as a nucleic acid nucleophile, to form, for example, a 7-alkylated guanidinium species.
  • suitable leaving groups include the halogens and the sulfonates (--SO 2 R).
  • the compound is a "mixed" leaving group compound, including two different types of leaving groups, for example a halogen and a sulfonate or two different halogens, such as a bromide and a chloride.
  • two different types of leaving groups for example a halogen and a sulfonate or two different halogens, such as a bromide and a chloride.
  • U.S. Pat. No. 6,197,760 to Struck teaches methods for making such mixed leaving group compounds. //. Formulation of IPM salts and analogues thereof
  • An aspect of the disclosure includes pharmaceutical formulations, such as an oral dosage form, prepared for administration to a subject and which include a therapeutically effective amount of one or more of the IPM salts and analogues thereof disclosed herein or elsewhere.
  • the formulation may be in the form of a pill, a tablet or a capsule to be administered orally.
  • the formulation is in the form of a capsule for oral administration.
  • the formulation comprises a lubricant, a diluent and a disintegrant in addition to, e.g., admixed with, the IPM salt or analogue thereof.
  • the formulation may comprise, for example, 0.25-5% of a lubricant, up to 98% of a diluent such as from 80 to 98%, such as 85 to 95% such as about 90% of a diluent, and up to 90% of a disintegrant such as from 0.5 to 10%, such as from 0.5 to 5%, such as about 1% of a disintegrant by weight of the formulation.
  • the formulation may further comprise one or more additional diluents, disintegrants or lubricants and additional carriers.
  • an oral dosage form comprises from 1 to 250 mg of the compound of formula (E) such as from about 1 to about 100 mg or from about 10 mg to about 50 mg.
  • the formulation comprises from 5-25 mg of the compound of formula (E) such as about 5 mg, about 7.5 mg, about 10 mg, about 12 mg, about 15 mg, about 20 mg and about 25 mg.
  • the compound of formula (E) is the tris(hydroxymethyl)aminomethane (Tris) salt:
  • X and Y are independently selected from leaving groups, such as Cl, Br, or I, or a sulfonate, e.g., toluenesulfonate, methanesulfonate, 2,4,6- triisopropylbenzenesulfonate, or 2,4,6-trimethylbenzenesulfonate.
  • leaving groups such as Cl, Br, or I
  • a sulfonate e.g., toluenesulfonate, methanesulfonate, 2,4,6- triisopropylbenzenesulfonate, or 2,4,6-trimethylbenzenesulfonate.
  • the lubricant of the formulation may be selected from any one or more of talc; fumed silicon dioxide such as Aerosil, Cab-O-Sil, or Syloid; starch; calcium silicate; magnesium carbonate (heavy); magnesium oxide (heavy); magnesium lauryl sulfate, sodium lauryl sulfate, calcium stearate, sodium stearyl fumarate, polyethylene glycol 4000 and 6000, sodium benzoate, light mineral oil, hydrogenated vegetable oils, stearic acid, or glyceryl behenate.
  • the lubricant is magnesium stearate.
  • the lubricant of the formulation comprises the salt of a fatty acid, such as the salt of a long chain, e.g., C10-C24, saturated or unsaturated fatty acid.
  • the salt of a fatty acid is a metallic salt, such as the magnesium salt of a fatty acid, e.g., magnesium stearate.
  • the lubricant of the formulation comprises a long chain fatty acid ester such as sodium stearyl fumarate.
  • the lubricant comprises a mixture of glycerides of fatty acids such as glyceryl behenate.
  • the formulation may comprise at least one of the following lubricants in the indicated amount (by weight of the formulation): Talc 1-5%,
  • the formulation comprises magnesium stearate in an amount
  • the capsule formulation may comprise a diluent selected from any one or more of lactose, microcrystalline cellulose, mannitol, calcium hydroxy-dioxido-oxo- phosphorane, dextrose, glucose, sucrose, starch and derivatives, calcium carbonate, dicalcium phosphate and magnesium carbonate.
  • the diluent is selected from microcrystalline cellulose, mannitol, lactose and calcium hydroxydiodioxido-oxo-phosphorane.
  • the diluent is microcrystalline cellulose.
  • the diluent comprises a carbohydrate, such as sugar or sugar alcohols (e.g., lactose, ⁇ -lactose monohydrate, sucrose, mannitol, or sorbitol), or a cellulose polymer such as microcrystalline cellulose, silicified microcrystalline cellulose, or powdered cellulose.
  • a carbohydrate such as sugar or sugar alcohols (e.g., lactose, ⁇ -lactose monohydrate, sucrose, mannitol, or sorbitol)
  • a cellulose polymer such as microcrystalline cellulose, silicified microcrystalline cellulose, or powdered cellulose.
  • the formulation may comprise at least one diluent in an amount up to 98% by weight of the formulation such as from about 50-85% or about 50-75%.
  • the formulation comprises one or more of the following diluents in the indicated amount by weight of the formulation: microcrystalline cellulose 5-98%, mannitol 10-90%, dextrose up to 98%, glucose up to 98%, starch and derivatives up to 98%, calcium carbonate up to 98%, dicalcium phosphate up to 98%, magnesium carbonate up to 98%, lactose up to 98% and calcium hydroxydiodioxido-oxo-phosphorane 10-80%.
  • the formulation comprises from 85-95% microcrystalline cellulose.
  • the formulation may comprise from 88-92% microcrystalline cellulose such as about 91% microcrystalline cellulose.
  • the formulation comprises 0.25-1% magnesium stearate and about 91% microcrystalline cellulose.
  • the formulation comprises about 91% microcrystalline cellulose and about 0.5% magnesium stearate.
  • the formulation may comprise at least one disintegrant, e.g., a water-soluble polymer, preferably an anionic water-soluble polymer, such as cellulose or a derivative thereof or a salt thereof.
  • the disintegrant may be selected from any one or more of starch, microcrystalline cellulose, insoluble ion exchange resins, sodium starch glycolate, sodium carboxymethylcellulose, gums such as agar, guar and xanthan, alginic acid, sodium alginate and povidone.
  • the disintegrant comprises a salt of cellulose or a derivative thereof.
  • Derivatives of cellulose include molecules in which one or more of the hydroxyl functionalities of cellulose are bound to atoms or groups of atoms other than hydrogen.
  • the disintegrant may comprise carboxymethylcellulose (CMC) (e.g., a cellulose derivative with carboxymethyl groups (-CH 2 -COOH) bound to some of the hydroxyl groups of the glucopyranose monomers that make up the cellulose backbone) or an anionic form thereof.
  • CMC carboxymethylcellulose
  • the disintegrant is or comprises sodium carboxymethylcellulose, which may optionally be crosslinked.
  • the disintegrant is selected such that the formulation disintegrates in the stomach in less than 30 minutes, such as less than 15 minutes, or even less than 10 minutes.
  • the formulation may comprise at least one disintegrant in an amount up to 90% by weight of the formulation.
  • the formulation comprises one of the following disintegrants in the indicated amount by weight of the formulation: microcrystalline cellulose 5-90%, starch 3-25%, sodium starch glycolate 2-8%, sodium carboxymethylcellulose up to 15%, gum less than 5% alginic acid or sodium alginate 4-6%, and crospovidone 1-5%.
  • the disintgrant is sodium carboxymethylcellulose.
  • the formulation may comprise from 0.5-2% sodium carboxymethylcellulose. In certain embodiments, the formulation comprises about 1% sodium carboxymethylcellulose. In certain embodiments, the formulation comprises 0.5-2.0% sodium carboxymethylcellulose, 0.25-1% magnesium stearate, at least about 90% microcrystalline cellulose, and from 5-9% of the compound of formula (E). In exemplary embodiments, the formulation comprises about 1% sodium carboxymethylcellulose, about 91% microcrystalline cellulose, about 0.5% magnesium stearate and about 15 mg of the compound of formula (E):
  • the formulation may further comprise one or more additional carriers such as a binder from 3-90% and a compression filler up to 98%.
  • the formulation may further comprise a carrier selected from a second diluent, a second disintegrant, and a second lubricant.
  • Other pharmaceutically acceptable carriers useful for these formulations are conventional. Remington 's Pharmaceutical Sciences, by E. W. Martin, Mack Publishing Co., Easton, PA, 19th Edition (1995), describes formulations suitable for pharmaceutical delivery of the compounds herein disclosed.
  • the formulation comprises a component that performs the function of two or more of a lubricant, a diluent, and a disintegrant, e.g., acts as both a lubricant and a disintegrant.
  • the formulation may comprise micro crystalline cellulose as both the diluent and the disintegrant.
  • there may or may not be one or more additional diluents and/or disintegrants in a formulation, and/or the multi-acting component is present in an amount equal to the amounts of all of the components whose functions it performs.
  • a single component of the formulation may act as all three of a diluent, a lubricant and a disintegrant.
  • each of a lubricant, diluent and disintegrant are compounds that are distinct from one another.
  • compositions can also include one or more additional active ingredients such as antimicrobial agents, anti-inflammatory agents, anesthetics, and the like.
  • certain embodiments of pharmaceutical formulations are formulated into unit dosage forms.
  • such unit dosage forms can contain from about 1 mg to about 250 mg, such as from about 5 mg to about 100 mg, such as about 5 mg to about 50 mg, such as about 5 mg, about 10 mg, about 15 mg, about 20 mg, about 25 mg, about 30 mg, about 35 mg, about 40 mg, about 45 mg or about 50 mg of a disclosed isophosphoramide mustard salt or analog thereof per dosage unit.
  • the formulations of IPM salts or analogs thereof disclosed herein are stable at room temperature for at least two weeks, at least one month, at least two months at 5 0 C, at least three months at 5 0 C, at least six months at 5 0 C, at least 9 months at 5 0 C, at least 12 months at 5 0 C, at least 18 months at 5 0 C, or even at least 24 months at 5 0 C.
  • the active ingredient of such stable formulations undergoes less than 10% decomposition, preferably less than 5%, 2%, or even less than 1% decomposition, e.g., as measured by assaying for the presence of decomposition by-products such as phosphoric acid and its salts and substituted ethylamines, such as by HPLC or GC, for at least two weeks, at least one month, at least two months, at least three months, or even at least six months.
  • the stable formulations maintain >90%, >95%, or even >98% potency at room temperature for at least two weeks, at least one month, at least two months at 5 0 C, at least three months at 5 0 C, at least six months at 5 0 C, at least 9 months at 5 0 C, at least 12 months at 5 0 C, at least 18 months at 5 0 C, or even at least 24 months at 5 0 C, e.g., as determined by HPLC analysis.
  • stable means that the purity of the IPM salt or analog thereof after a period of time (e.g., one month, two months, three months, six months, one year, etc.) is at least 90%, at least 95%, at least 97%, or even at least 99% of the initial purity, which may be determined e.g., by HPLC using evaporative light scattering detection (ELSD).
  • ELSD evaporative light scattering detection
  • Such an assay may be performed, for example, using a Cl 8 column and an isocratic system with a mobile phase comprising 0.005 M heptafluorobutyric acid and 0.1% trifluoroacetic acid in water.
  • compositions that can be used orally include push-fit capsules made of gelatin (“gelcaps”), as well as soft, sealed capsules made of gelatin, and a plasticizer, such as glycerol or sorbitol.
  • the push-fit capsules can contain the active ingredients in admixture with carriers.
  • the active compounds may be dissolved or suspended in suitable liquids, such as fatty oils, liquid paraffin, or liquid polyethylene glycols (PEGs).
  • suitable liquids such as fatty oils, liquid paraffin, or liquid polyethylene glycols (PEGs).
  • PEGs liquid polyethylene glycols
  • stabilizers may be added.
  • Neoplasia refers to the process of abnormal and uncontrolled cell growth. Neoplasia is one example of a proliferative disorder.
  • the product of neoplasia is a neoplasm (a tumor), which is an abnormal growth of tissue that results from excessive cell division. A tumor that does not metastasize is referred to as "benign.” A tumor that invades the surrounding tissue and/or can metastasize is referred to as "malignant.”
  • Conditions that can be treated according to the disclosed method include those characterized by abnormal cell growth and/or differentiation, such as cancers and other neoplastic conditions. Typical examples of proliferative disorders that can be treated using the disclosed compounds and formulations are listed below.
  • leukemias examples include leukemias, including acute leukemias (such as acute lymphocytic leukemia, acute myelocytic leukemia, acute myelogenous leukemia and myeloblastic, promyelocytic, myelomonocytic, monocytic and erythroleukemia), chronic leukemias (such as chronic myelocytic (granulocytic) leukemia, chronic myelogenous leukemia, and chronic lymphocytic leukemia), polycythemia vera, lymphoma, Hodgkin's disease, non-Hodgkin's lymphoma (indolent and high grade forms), multiple myeloma, Waldenstrom's macroglobulinemia, heavy chain disease, myelodysplasia syndrome, hairy cell leukemia and myelodysplasia.
  • acute leukemias such as acute lymphocytic leukemia, acute myelocytic leukemia, acute my
  • solid tumors such as sarcomas and carcinomas
  • solid tumors include fibrosarcoma, myxosarcoma, liposarcoma, chondrosarcoma, osteogenic sarcoma, and other sarcomas, synovioma, mesothelioma, E wing's tumor, leiomyosarcoma, rhabdomyosarcoma, colon carcinoma, lymphoid malignancy, pancreatic cancer, breast cancer, lung cancers, ovarian cancer, prostate cancer, hepatocellular carcinoma, squamous cell carcinoma, basal cell carcinoma, adenocarcinoma, sweat gland carcinoma, sebaceous gland carcinoma, papillary carcinoma, papillary adenocarcinomas, medullary carcinoma, bronchogenic carcinoma, renal cell carcinoma, hepatoma, bile duct carcinoma, choriocarcinoma, Wilms' tumor, cervical cancer,
  • the methods disclosed herein include treating a subject having a CPA-resistant neoplastic condition with an isophosphoramide mustard salt or analog thereof as disclosed herein.
  • a subject is administered from about 0.2 mg/kg/day to about 20 mg/kg/day of a disclosed isophosphoramide mustard salt or analog thereof.
  • a disclosed isophosphoramide mustard salt or analog thereof For example, from about 0.5 to about 10 mg/kg/day, such as from about 1 to about 7.5 mg/kg/day of a disclosed compound can be administered to a subject.
  • a subject is administered from about 10 to about 700 mg/m 2 /day, such as from about 20 to about 400 mg/m 2 /day or from about 100 to about 500 mg/m 2 /day. For example, from about 30 to about 100 mg/m 2 /day, such as from about 40 to about 90 mg/m 2 /day of a compound disclosed herein.
  • a disclosed compound is administered to a subject on a multiple daily dosing schedule.
  • the compound is administered on at least two days and on as many as five different days.
  • the compound is administered to the subject on consecutive days, such as from two to five consecutive days.
  • one or more additional therapeutic agents is administered to a subject in addition to the presently disclosed compounds and formulations.
  • additional therapeutic agents can that can be used include microtubule binding agents, DNA intercalators or cross-linkers, DNA synthesis inhibitors, DNA and/or RNA transcription inhibitors, antibodies, enzymes, enzyme inhibitors, gene regulators, and/or angiogenesis inhibitors.
  • Microtubule binding agent refers to an agent that interacts with tubulin to stabilize or destabilize microtubule formation thereby inhibiting cell division.
  • microtubule binding agents that can be used in conjunction with the presently disclosed isophosphoramide mustard salts and analogs thereof include, without limitation, paclitaxel, docetaxel, vinblastine, vindesine, vinorelbine (navelbine), the epothilones, colchicine, dolastatin 15, nocodazole, podophyllotoxin and rhizoxin. Analogs and derivatives of such compounds also can be used and will be known to those of ordinary skill in the art.
  • epothilones and epothilone analogs for incorporation into the present compounds are described in International Publication No. WO 2004/018478, which is incorporated herein by reference.
  • Taxoids such as paclitaxel and docetaxel are currently believed to be particularly useful as therapeutic agents in the presently disclosed compounds. Examples of additional useful taxoids, including analogs of paclitaxel are taught by U.S. Patent Nos. 6,610,860 to Holton, 5,530,020 to Gurram et al. and 5,912,264 to Wittman et al. Each of these patents is incorporated herein by reference.
  • Suitable DNA and/or RNA transcription regulators including, without limitation, actinomycin D, daunorubicin, doxorubicin and derivatives and analogs thereof also are suitable for use in combination with the presently disclosed compounds.
  • DNA intercalators and cross-linking agents that can be incorporated into the disclosed compounds include, without limitation, cisplatin, carboplatin, oxaliplatin, mitomycins, such as mitomycin C, bleomycin, chlorambucil, cyclophosphamide and derivatives and analogs thereof.
  • DNA synthesis inhibitors suitable for use as therapeutic agents include, without limitation, methotrexate, 5-fluoro-5'-deoxyuridine, 5-fluorouracil and analogs thereof.
  • Suitable enzyme inhibitors for use in combination with the presently disclosed compounds include, without limitation, camptothecin, etoposide, formestane, trichostatin and derivatives and analogs thereof.
  • Suitable therapeutics for use with the presently disclosed compounds that affect gene regulation include agents that result in increased or decreased expression of one or more genes, such as, without limitation, raloxifene, 5-azacytidine, 5-aza-T- deoxycytidine, tamoxifen, 4-hydroxytamoxifen, mifepristone and derivatives and analogs thereof.
  • angiogenesis inhibitor is used herein, to mean a molecule including, but not limited to, biomolecules, such as peptides, proteins, enzymes, polysaccharides, oligonucleotides, DNA, RNA, recombinant vectors, and small molecules that function to inhibit blood vessel growth.
  • Angiogenesis is implicated in certain pathological processes, such as those involved in disorders such as diabetic retinopathy, chronic inflammatory diseases, rheumatoid arthritis, dermatitis, psoriasis, stomach ulcers, and most types of human solid tumors.
  • Angiogenesis inhibitors are known in the art and examples of suitable angiogenesis inhibitors include, without limitation, angiostatin Kl -3, staurosporine, genistein, fumagillin, medroxyprogesterone, suramin, interferon-alpha, metalloproteinase inhibitors, platelet factor 4, somatostatin, thromobospondin, endostatin, thalidomide, and derivatives and analogs thereof.
  • therapeutic agents particularly anti-tumor agents, that may or may not fall under one or more of the classifications above, also are suitable for administration in combination with the presently disclosed compounds.
  • such agents include adriamycin, apigenin, rapamycin, zebularine, cimetidine, and derivatives and analogs thereof.
  • the methods are used to prepare compounds of Formula (E):
  • X and Y independently represent leaving groups
  • a + is an ammonium cation.
  • the present disclosure provides methods for preparing compounds of Formula (E) via the pathway in Scheme 1.
  • phosphine oxide (A) is treated with alcohol R 1 OH affording monoester (B).
  • Monoester (B) is treated with one or more amines, e.g., XCH 2 CH 2 NH 2 and YCH2CH2NH2 or salts thereof in concert or in series, under condensation conditions affording phosphordiamidate (C).
  • Phosphordiamidate (C) is converted under hydrogeno lysis conditions to phosphordiamidic acid (D).
  • Phosphordiamidic acid (D) is then converted to a salt by treatment with a base.
  • the present invention provides a method for the preparation of a compound of formula (B): fl
  • X 1 independently for each occurrence, is selected from Cl, I, and Br,
  • R 1 is benzyl, optionally substituted with one or more substituents, e.g., selected from halogen, -R 2 , -OR 2 and -NR 2 2 , wherein R 2 is independently selected for each occurrence from H and lower alkyl.
  • R 1 is benzyl optionally substituted with one or more substituents. In certain embodiments, R 1 is unsubstituted benzyl. In certain embodiments, X 1 at each occurrence is independently selected from any of -Cl, -Br and -I. In certain embodiments, the compound of formula (A) is P(0)Cl3 and/or R 1 OH is PhCH 2 OH .
  • the condensation conditions comprise an amine base.
  • the amine base is selected from any of N-methyl morpholine, triethylamine, pyridine or diisopropylethylamine, e.g., triethylamine.
  • the condensation conditions may comprise an aprotic organic solvent, e.g., acetone, 2-butanone, butyl acetate, ethyl acetate, acetonitrile, toluene, THF, dioxane, N 5 N-DMF, DMSO, 1 ,2-dichloroethane, or methylene chloride.
  • the aprotic organic solvent comprises acetonitrile, wherein the acetonitrile may represent, for example, more than about 10, 20, 30, 50, 70, or 90% of the solvent system, or substantially all of the solvent system, for example about 95% or greater of the solvent system.
  • phosphine oxide A and R 1 OH are combined under condensation conditions, e.g. , in a ratio in the range of 2 : 1 to 1 : 1.2 of compound of formula (A) to R 1 OH, such as in a ratio in the range of 1.2: 1 to 1 : 1.2, preferably approximately equimolar amounts of the compound of formula (A) and alcohol R 1 OH.
  • the condensation conditions comprise maintaining a reduced temperature, e.g., in the range of about -50 to about -10 0 C, such as from about -35 to about -25 0 C, e.g., about -30 0 C.
  • the present invention provides a method for the preparation of a compound of formula (C):
  • X and Y independently represent leaving groups which may be the same or different
  • R 1 is benzyl optionally substituted with one or more substituents, e.g., selected from halogen, -R 2 , -OR 2 and -NR 2 2 , wherein R 2 is independently selected for each occurrence from H and lower alkyl.
  • R 1 is benzyl optionally substituted with one or more substituents. In certain embodiments, R 1 is unsubstituted benzyl. In certain embodiments, X 1 at each occurrence is independently selected from any of Cl, Br and I. In certain embodiments, R 1 is unsubstituted benzyl and/or X 1 is selected at each occurrence from Cl or Br.
  • X and Y of amines XCH 2 CH 2 NH 2 and YCH 2 CH 2 NH 2 may be independently selected from halogen, e.g., Cl, Br, or I, or a sulfonate, e.g., toluenesulfonate, methanesulfonate, 2,4,6-triisopropylbenzenesulfonate, or 2,4,6- trimethylbenzenesulfonate.
  • X and Y are independently selected from Cl, Br or I.
  • X and Y are identical, e.g., X and Y are both Cl.
  • XCH 2 CH 2 NH 2 and YCH 2 CH 2 NH 2 may be employed in the form of salts such as the HCl salt.
  • the amine or amines may be introduced to the compound of formula (B) in a single dose, in portions over time, or in multiple smaller doses.
  • the amine is steadily added to the compound of formula (B) over a period of time, e.g., with a continuous feed, a syringe pump or an addition funnel.
  • the amines e.g., ClCH 2 CH 2 NH 2 and BrCH 2 CH 2 NH 2
  • the amines can be introduced to a compound of formula (B) in concert or, preferably, in series.
  • the amine ClCH 2 CH 2 NH 2 is introduced to the compound of formula (B) in one dose and, e.g., after reacting to completion, amine BrCH 2 CH 2 NH 2 is added.
  • the sum of molar equivalents of amines XCH 2 CH 2 NH 2 and YCH 2 CH 2 NH 2 relative to the compound of formula (B) is a ratio in the range of 2.5 : 1 to 1.8 : 1.
  • the ratio of amine components to the compound of formula (B) is approximately 2:1.
  • amines XCH 2 CH 2 NH 2 and YCH 2 CH 2 NH 2 are approximately equimolar to each other, and together are added in a ratio of approximately 2:1 relative to the compound of formula (B).
  • the condensation conditions may comprise an amine base such as N-methyl morpholine, triethylamine, pyridine or diisopropylethylamine.
  • the amine base is in a ratio of 5:1 to 3:1 relative to the compound of formula (B).
  • the amine base is in a ratio of approximately 4:1 relative to the compound of formula (B).
  • the amine base may be triethylamine in a ratio of 4:1 relative to the compound of formula (B). It will be recognized by those of skill in the art that more amine base will be advantageous when amines XCH 2 CH 2 NH 2 and YCH 2 CH 2 NH 2 are added in their salt form than if they are added in their free-base form.
  • the condensation reaction will be facilitated by the addition of two or more equivalents of amine base when XCH 2 CH 2 NH 2 and YCH 2 CH 2 NH 2 are used in their free-base form, whereas four or more equivalents of amine base are preferred when XCH 2 CH 2 NH 2 and YCH 2 CH 2 NH 2 are added as amine salts.
  • the present invention provides a method for the preparation of a compound of formula (C):
  • X and Y independently represent leaving groups
  • X 1 independently for each occurrence, is selected from Cl, I, and Br,
  • R 1 is benzyl optionally substituted with one or more substituents, e.g., selected from halogen, -R 2 , -OR 2 and -NR 2 2 , wherein R 2 is independently selected for each occurrence from H and lower alkyl.
  • R 1 is benzyl optionally substituted with one or more substituents. In certain embodiments, R 1 is unsubstituted benzyl. In certain embodiments, X 1 at each occurrence is independently selected from any of Cl, Br and I. In certain embodiments, R 1 is unsubstituted benzyl and/or X 1 is selected at each occurrence from Cl or Br, e.g., the compound of formula (A) may be P(0)Cl3.
  • the condensation conditions comprise an amine base. In certain such embodiments, the amine base is selected from any of N-methyl morpholine, triethylamine, pyridine or diisopropylethylamine, e.g., triethylamine.
  • the condensation conditions may comprise an aprotic organic solvent, e.g., one or more of acetone, 2-butanone, butyl acetate, ethyl acetate, acetonitrile, toluene, THF, dioxane, N 5 N-DMF, DMSO, 1 ,2-dichloroethane, or methylene chloride.
  • the aprotic solvent comprises acetonitrile, wherein the acetonitrile may represent, for example, more than about 10, 20, 30, 50, 70, or 90% of the solvent system, or substantially all of the solvent system, for example about 95% or greater of the solvent system.
  • phosphine oxide (A) and R 1 OH are combined under condensation conditions, e.g. , in a ratio in the range of 2 : 1 to 1 : 1.2 of compound of formula (A) to R 1 OH, such as in a ratio in the range of 1.2: 1 to 1 : 1.2, e.g., in approximately equimolar amounts of the compound of formula (A) and substitution reagent R 1 OH.
  • the condensation conditions comprise maintaining an reduced temperature, e.g., in the range of about -50 to about -10 0 C, or from about -35 to about -25 0 C, or about -30 0 C.
  • X and Y of amines XCH 2 CH 2 NH 2 and YCH 2 CH 2 NH 2 may be independently selected from halogen, e.g., Cl, Br, or I or a sulfonate, e.g., toluenesulfonate, methanesulfonate, 2,4,6-triisopropylbenzenesulfonate, or 2,4,6- trimethylbenzenesulfonate.
  • X and Y are independently selected from Cl, Br or I.
  • X and Y are identical, e.g., both Cl.
  • XCH 2 CH 2 NH 2 and YCH 2 CH 2 NH 2 may be employed in the form of salts, such as the HCl salt.
  • the amine may be introduced to the reaction mixture in a one-time dose, in portions over time, or in multiple smaller doses.
  • the amine is steadily added to the compound of formula (B) over a period of time, e.g., with a syringe pump, an addition funnel, or continuous feed.
  • X and Y of amines XCH 2 CH 2 NH 2 and YCH 2 CH 2 NH 2 are distinct from one another, e.g., X is Cl and Y is Br, or X is Br and Y is I
  • the amines e.g., ClCH 2 CH 2 NH 2 and BrCH 2 CH 2 NH 2
  • the amines may be introduced to the reaction mixture in concert or, preferably, in series.
  • the amine ClCH 2 CH 2 NH 2 is introduced to the reaction mixture in one dose and, e.g., after reacting to completion, amine BrCH 2 CH 2 NH 2 is added.
  • the sum of molar equivalents of amines XCH 2 CH 2 NH 2 and YCH 2 CH 2 NH 2 relative to the compound of formula (A) are in a ratio in the range of 2.5:1 to 1.8:1.
  • the ratio of amine components to the compound of formula (A) is approximately 2:1.
  • amines XCH 2 CH 2 NH 2 and YCH 2 CH 2 NH 2 are approximately equimolar to each other, and together are added in a ratio of approximately 2:1 relative to compound of formula (A).
  • the condensation conditions may comprise an amine base such as N-methyl morpholine, triethylamine, pyridine or diisopropylethylamine.
  • the amine base is in a ratio of 5:1 to 3:1 relative to the compound of formula (A).
  • the amine base is in a ratio of approximately 4:1 relative to the compound of formula (A).
  • the amine base may be triethylamine in a ratio of 4:1 relative to the compound of formula (A). It will be recognized by those of skill in the art that more amine base will be advantageous when amines XCH 2 CH 2 NH 2 and YCH 2 CH 2 NH 2 are added in their salt form than if they are added in their free-base form.
  • condensation reaction will be facilitated by the addition of two or more equivalents of amine base when XCH 2 CH 2 NH 2 and YCH 2 CH 2 NH 2 are used in their free-base form, whereas four or more equivalents of amine base are preferred when XCH 2 CH 2 NH 2 and YCH 2 CH 2 NH 2 are added as amine salts (in addition to any amine base used in the condensation with alcohol R 1 OH, e.g., typically at least one further equivalent).
  • the reaction mixture comprising the product of the reaction of the compound of formula (B) to form the compound of formula (C) is used in the hydrogenolysis reaction, e.g., without first purifying or partially or completely removing solvents from the reaction mixture.
  • the reaction mixture may be filtered to remove solids, e.g., salt by-products of the condensation conditions, prior to subjecting the solution to the hydrogeno lysis conditions affording the compound of formula (D).
  • the reaction mixture may be filtered by any method known in the art to remove solids from the solvent of the reaction mixture.
  • the reaction mixture is filtered and substantially directly subjected to hydrogenation conditions, e.g., the compound of formula (C) is not further purified or isolated from the reaction mixture (e.g., no extractions, chromatography, or quenches are performed).
  • the present invention provides a method for the preparation of a compound of formula (D):
  • X and Y independently represent leaving groups
  • R 1 is benzyl optionally substituted with one or more substituents, e.g., selected from halogen, -R 2 , -OR 2 and -NR 2 2 , wherein R 2 is independently selected for each occurrence from H and lower alkyl.
  • R 1 is benzyl optionally substituted with one or more substituents. In certain embodiments, R 1 is unsubstituted benzyl. In certain embodiments, X and Y at each occurrence are independently selected from halogens such as Cl, Br and I. In certain embodiments, R 1 is unsubstituted benzyl and/or X and Y are both CL
  • the reaction mixture comprising the product of the reaction of the compound of formula (B) to form the compound of formula (C) is used in the hydrogenolysis reaction, e.g., without first purifying or partially or completely removing solvents from the reaction mixture.
  • the reaction mixture may be filtered to remove solids, e.g., salt by-products of the condensation conditions, prior to subjecting the solution to the hydrogenolysis conditions affording the compound of formula (D).
  • the reaction mixture may be filtered by any method known in the art to remove solids from the solvent of the reaction mixture.
  • the reaction mixture is filtered and substantially directly subjected to hydrogenation conditions, e.g., the compound of formula (C) is not further purified or isolated from the reaction mixture (e.g., no extractions, chromatography or quenches are performed).
  • the hydrogenolysis conditions may comprise treating the compound of formula (C) with hydrogen gas in the presence of a catalyst.
  • the catalyst may be selected from any suitable hydrogenolysis catalyst, such as Pd/carbon, Pd black, Pd EnCat (polymer encapsulated active metal catalyst) Raney nickel, Rh/carbon, Ru/carbon, Re/carbon, palladium oxide, palladium chloride, PtO 2 or RuO 2 .
  • the hydrogenolysis catalyst comprises palladium, e.g., Pd/carbon.
  • the hydrogenolysis conditions comprise a partial pressure of hydrogen greater than 1 atmosphere.
  • the partial pressure of hydrogen is less than or equal to 100, 75 or 50 psi.
  • the partial pressure of hydrogen is selected from between 10 psi and 50 psi.
  • the partial pressure of hydrogen may be from 20-50 psi, such as from 40-50 psi.
  • the partial pressure of hydrogen during hydrogenolysis may be about 50 psi, or even between 50 and 75 psi.
  • the hydrogenolysis conditions may comprise an aprotic organic solvent, e.g., toluene, xylene, benzene, furan, acetonitrile, dioxane, tetrahydrofuran, chloroform or mixtures thereof.
  • the aprotic solvent comprises acetonitrile, wherein the acetonitrile may represent, for example, more than about 10, 20, 30, 50, 70, or 90% of the solvent system, or substantially all of the solvent system, for example about 95% or greater of the solvent system.
  • the separation of the product from residual catalyst is achieved by the formation of a basic salt under aqueous conditions, e.g., using sodium hydroxide or another base in water, which may be performed in situ.
  • the resulting salt may be dissolved in a suitable solvent and the residual catalyst may be filtered to remove solids from the solvent of the reaction mixture.
  • the separation of the product from residual catalyst is achieved by the formation of a basic salt under anhydrous conditions, e.g., using triethylamine or another base, e.g., an amine base, preferably a sterically hindered base such as diisopropylethylamine or proton sponge.
  • the subsequent salt may be dissolved into the reaction solvent and the residual catalyst may be filtered to remove solids from the solvent of the reaction mixture.
  • the present invention provides a method for the preparation of a compound of formula (E):
  • X and Y independently represent leaving groups; and
  • a + represents an ammonium cation.
  • X and Y at each occurrence are independently selected from halogens such as -Cl, -Br and -I. In certain embodiments, X and Y are both Cl.
  • a + represents BH + and B is an amine selected from the basic amino acids, pyridine, N, ⁇ /-dimethylaminopyridine, diazabicyclononane, diazabicycloundecene, ⁇ /-methyl-JV-ethylamine, diethylamine, triethylamine, diisopropylethylamine, mono-, bis- or tris-(2-hydroxyethyl)amine, 2-hydroxy-tert- butylamine, tris(hydroxymethyl)methylamine, N,N-dimethyl-N-(2- hydroxyethyl)amine, tri-(2-hydroxyethyl)amine and N-methyl-D-glucamine.
  • B is tris(hydroxymethyl)methylamine.
  • the salt-forming conditions comprise combining approximately equimolar amounts of an amine base and the compound of formula (D). In certain embodiments the compound of formula (D) and the amine base are combined in a molar ratio in the range of 1 : 1 to 1 : 10. In certain embodiments, the salt- forming conditions comprise combining approximately equimolar amounts of tris(hydroxymethyl)aminomethane and the compound of formula (D).
  • the salt-forming conditions comprise a polar aprotic solvent, such as N 5 N-DMF, acetone, DMSO, THF, 2-butanone, butyl acetate, ethyl acetate, acetonitrile, and combinations thereof.
  • the aprotic solvent comprises N 5 N-DMF, wherein the N 5 N-DMF may represent, for example, more than about 10, 20, 30, 50, 70, or 90% of the solvent system, or substantially all of the solvent system, for example about 95% or greater of the solvent system.
  • the invention relates to a compound comprising a crystalline salt of IPM or analog thereof wherein the IPM or analog thereof, and the counterion, preferably tris (hydroxymethyl) amino methane (tris), are present in a ratio from 2: 1 to 1 :2, preferably 1 :1.
  • the crystalline formulation comprises more than one polymorphic form of crystals, such as two, three, four, or even five polymorphic forms of crystals.
  • the crystalline formulation comprises a single polymorphic form of crystals.
  • such salts are more stable than IPM and IPM analogs as free acids.
  • the compound is a crystalline salt of a 1 :1 ratio of IPM and Tris.
  • the melting point of the crystalline solid is between about 100 and about 110 0 C, about 102 to about 108 0 C, about 103 to about 106 0 C, or even 105 to 106 0 C.
  • the compound e.g., a crystalline salt of a 1 :1 ratio of IPM and Tris
  • the compound is at least about 80% pure, at least about 85% pure, at least 90% pure, at least 95% pure, at least 97% pure, at least 98% pure, or even at least 99% pure.
  • no single impurity exceeds 1% by weight.
  • purity is measured relative to all other components of the formulation, while in other embodiments (e.g., where the compound is part of a pharmaceutical formulation or lyophilisate mixture), purity may be measured relative to degradation products of the compound (e.g., phosphorous-containing degradation products of the compound) or by-products of the manufacture of the compound (e.g., phosphorous- containing degradation products of the compound), thereby excluding other components purposefully added to the formulation.
  • degradation products of the compound e.g., phosphorous-containing degradation products of the compound
  • by-products of the manufacture of the compound e.g., phosphorous- containing degradation products of the compound
  • IPM tris drug formulation comprises a blend of IPM tris salt, Microcrystalline Cellulose (Avicel PHl 12), Sodium Croscarmellose (Ac-Di-SoI) and Magnesium Stearate (vegetable source).
  • API active pharmaceutical ingredient
  • NA not available
  • NF National
  • CTM clinical trials material
  • HPLC high-performance liquid chromatography
  • ND not detected
  • RRT relative retention time
  • NA not available
  • HPLC high-performance liquid chromatography
  • ND not detected
  • RRT relative retention time
  • NA not available
  • CTM clinical trials material
  • HPLC high-performance liquid chromatography
  • ND not detected
  • RRT relative retention time
  • NA not available
  • the resulting mixture was filtered to remove catalyst and rinsed with 2 x 100 mL of acetonitrile.
  • the filtrate was cooled to O 0 C to 1O 0 C, and to it 76 mL (924.5 mmol, 1.4 equiv) of 37% HCl was added to lower the pH to 1-2 (Note: This addition took 15 min).
  • the resulting slurry was filtered and the wet cake was made into a slurry with two portions of 400 mL of 5% water in acetonitrile, and stirred for 5 min each.
  • the wet cake was then rinsed with 3 x 200 mL of acetonitrile to give 105.8871 g (73.5%) product.
  • the resulting solution proceeds polish filtration with Whatman #1 filter paper.
  • the filtrate was transferred into a 2 L flask, and to it, 144 mL of acetonitrile was added over 5 min.
  • 852 mL of methyl tert-butyl ether (MTBE) was introduced to form cloudy solution (Solid seeds were generated by scratching against the glass wall with a spatula).
  • the batch was stirred for 1 h.
  • the product was collected by filtration, followed by washing with 242 mL of MTBE in a yield of 72.3868 g (96.4%) as white solid. Residual palladium content was ⁇ 10ppm by ICP analysis.
  • IPM salt (L) Into a 500 mL 3-neck flask, 54.1043 g of tris(hydroxymethyl)-aminomethane was added, followed by addition of 158 mL of NJV-OMF. The mixture was then heated to 100 0 C to dissolve the base. After a clear solution formed, the batch was cooled to 20-25 0 C (a slurry then formed). To the above slurry, 100.0135 g (98.7% purity based on NMR, 0.4466 moles) of IPM (1766-028-11) was weighed, and rinsed with 99 mL of N 5 N-DMF. The mixture was stirred for 140 min until a clear solution formed.
  • the resulting solution proceeds polish filtration with Whatman #1 filter paper.
  • the filtrate was transferred into a 5 L flask, and to it, 293 mL of acetonitrile was added over 5 min.
  • a slurry mixture of 0.3 g of salt L in 4.8 mL of DMF and 5.7 mL of acetonitrile was added.
  • 1734 mL of MTBE was introduced. The batch was stirred for 1 h.
  • the product was collected by filtration, followed by washing with 494 mL of MTBE in a yield of 146.7 g (96.0%) as white solid.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Molecular Biology (AREA)
  • Biochemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Cardiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nutrition Science (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Engineering & Computer Science (AREA)
  • Inorganic Chemistry (AREA)
  • Physiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Peptides Or Proteins (AREA)
  • Saccharide Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

L'invention porte sur des formulations et des procédés de fabrication de composés de formule (E) : dans laquelle X et Y représentent indépendamment des groupes partants ; et A+ est un cation ammonium.
PCT/US2009/052295 2008-07-31 2009-07-30 Synthèse et formulations de sels de moutarde d'isophosphoramide et de leurs analogues WO2010014841A1 (fr)

Priority Applications (15)

Application Number Priority Date Filing Date Title
JP2011521338A JP5711660B2 (ja) 2008-07-31 2009-07-30 イソホスホルアミドマスタードの塩およびその類似体の合成および製剤
EP09803607.2A EP2318013A4 (fr) 2008-07-31 2009-07-30 Synthèse et formulations de sels de moutarde d'isophosphoramide et de leurs analogues
CN200980133758XA CN102137674A (zh) 2008-07-31 2009-07-30 异磷酰胺芥及其类似物的合成和制剂
MX2011001122A MX2011001122A (es) 2008-07-31 2009-07-30 Sintesis y formulaciones de sales de mostaza de isofosforoamida y analogos de las mismas.
EA201170277A EA022655B1 (ru) 2008-07-31 2009-07-30 Синтез и составы на основе солей изофосфорамидного иприта и его аналогов
BRPI0916739A BRPI0916739A2 (pt) 2008-07-31 2009-07-30 síntese e formulações de sais de mostarda de isofosforamida e análogos dos mesmos
CA2732290A CA2732290A1 (fr) 2008-07-31 2009-07-30 Synthese et formulations de sels de moutarde d'isophosphoramide et de leurs analogues
US13/056,628 US8664201B2 (en) 2008-07-31 2009-07-30 Synthesis and formulations of salts of isophosphoramide mustard and analogs thereof
NZ590995A NZ590995A (en) 2008-07-31 2009-07-30 Oral formulations of salts of isophosphoramide mustard and its analogs and their use in the treatment of a condition characterised by abnormal cell growth or differentiation (such as cancer)
AU2009276512A AU2009276512B2 (en) 2008-07-31 2009-07-30 Synthesis and formulations of salts of isophosphoramide mustard and analogs thereof
IL210921A IL210921A (en) 2008-07-31 2011-01-27 Oral preparations of isoposporamide mustard salts for the treatment of aberrant cell growth
ZA2011/00878A ZA201100878B (en) 2008-07-31 2011-02-02 Synthesis and formulations of salts of isophosphoramide mustard and analogs thereof
US14/167,169 US9145431B2 (en) 2008-07-31 2014-01-29 Synthesis and formulations of salts of isophosphoramide mustard and analogs thereof
US14/806,720 US9254298B2 (en) 2008-07-31 2015-07-23 Synthesis and formulations of salts of isophosphoramide mustard and analogs thereof
US14/987,185 US20160215005A1 (en) 2008-07-31 2016-01-04 Synthesis and formulations of salts of isophosphoramide mustard and analogs thereof

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US13753808P 2008-07-31 2008-07-31
US61/137,538 2008-07-31

Related Child Applications (2)

Application Number Title Priority Date Filing Date
US13/056,628 A-371-Of-International US8664201B2 (en) 2008-07-31 2009-07-30 Synthesis and formulations of salts of isophosphoramide mustard and analogs thereof
US14/167,169 Continuation US9145431B2 (en) 2008-07-31 2014-01-29 Synthesis and formulations of salts of isophosphoramide mustard and analogs thereof

Publications (2)

Publication Number Publication Date
WO2010014841A1 true WO2010014841A1 (fr) 2010-02-04
WO2010014841A8 WO2010014841A8 (fr) 2011-02-17

Family

ID=41610732

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2009/052295 WO2010014841A1 (fr) 2008-07-31 2009-07-30 Synthèse et formulations de sels de moutarde d'isophosphoramide et de leurs analogues

Country Status (16)

Country Link
US (4) US8664201B2 (fr)
EP (1) EP2318013A4 (fr)
JP (2) JP5711660B2 (fr)
KR (1) KR20110038696A (fr)
CN (2) CN104490900A (fr)
AU (1) AU2009276512B2 (fr)
BR (1) BRPI0916739A2 (fr)
CA (1) CA2732290A1 (fr)
EA (1) EA022655B1 (fr)
IL (1) IL210921A (fr)
MX (1) MX2011001122A (fr)
NZ (3) NZ590995A (fr)
SG (2) SG10201600595PA (fr)
TW (1) TWI454266B (fr)
WO (1) WO2010014841A1 (fr)
ZA (1) ZA201100878B (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013116281A1 (fr) * 2012-01-31 2013-08-08 Ziopharm Oncology, Inc. Polythérapie à base de moutarde isophosphoramide, d'analogues, ou de sels de celle-ci
US8664201B2 (en) 2008-07-31 2014-03-04 Ziopharm Oncology, Inc. Synthesis and formulations of salts of isophosphoramide mustard and analogs thereof

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103172662A (zh) * 2004-10-25 2013-06-26 德克技术公司 作为抗肿瘤剂的异磷酰胺氮芥及其类似物的盐
ES2585935T3 (es) 2007-03-07 2016-10-10 Becton Dickinson And Company Conjunto de seguridad de recogida de sangre con indicador
US8888713B2 (en) 2007-03-07 2014-11-18 Becton, Dickinson And Company Safety blood collection assembly with indicator
US8603009B2 (en) 2008-03-07 2013-12-10 Becton, Dickinson And Company Flashback blood collection needle
CN102924507A (zh) * 2011-11-10 2013-02-13 安徽四维药业有限公司 一种抗肿瘤化合物及其制备方法与应用、药物组合物

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SU427945A1 (ru) * 1972-07-24 1974-05-15 Институт элементоорганических соединений СПОСОБ ПОЛУЧЕНИЯа ПОЛИФТОРАЛКИЛЗАМЕЩЕННЫХБЕНЗИЛДИХЛОРФОСФАТОВ
WO2006047575A2 (fr) * 2004-10-25 2006-05-04 Dekk-Tec Inc. Sels d'yperite d'isophosphoramide et analogues de ceux-ci utilises en tant qu'agents anti-tumoraux

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2130578A1 (fr) 1992-04-17 1993-10-28 Geewananda P. Gunawardana Derives de taxol
US5912264A (en) 1997-03-03 1999-06-15 Bristol-Myers Squibb Company 6-halo-or nitrate-substituted paclitaxels
AU773061B2 (en) * 1999-05-24 2004-05-13 Southern Research Institute Isophosphoramide mustard analogs and use thereof
AR030188A1 (es) 2000-02-02 2003-08-13 Univ Florida State Res Found Compuestos de taxano sustituidos con esteres en el c7; composiciones farmaceuticas que los contienen y proceso para tratar un sujeto mamifero que sufre de una condicion que responde a los taxanos
MXPA05002113A (es) 2002-08-23 2005-06-03 Sloan Kettering Inst Cancer Sintesis de epotilonas, intermediarios para ellas, analogos y usos de los mismos.
HUE025949T2 (en) * 2007-04-06 2016-05-30 Ziopharm Oncology Inc Salts of isophosphoramide mustard and analogues thereof
SG10201600595PA (en) 2008-07-31 2016-02-26 Ziopharm Oncology Inc Synthesis and formulations of salts of isophosphoramide mustard and analogs thereof

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SU427945A1 (ru) * 1972-07-24 1974-05-15 Институт элементоорганических соединений СПОСОБ ПОЛУЧЕНИЯа ПОЛИФТОРАЛКИЛЗАМЕЩЕННЫХБЕНЗИЛДИХЛОРФОСФАТОВ
WO2006047575A2 (fr) * 2004-10-25 2006-05-04 Dekk-Tec Inc. Sels d'yperite d'isophosphoramide et analogues de ceux-ci utilises en tant qu'agents anti-tumoraux

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 81:37378, XP008143854 *
HAN, S.Y. ET AL.: "Synthesis of O (and O) Labelled Isophosphoramide Mustard", JOURNAL OF LABELLED COMPOUNDS AND RADIOPHARMACEUTICALS, vol. XXXIV, no. 3, 1994, pages 247 - 254, XP008142829 *
MISIURA, K ET AL.: "'Isophosphoramide mustard analogues as prodrugs for anti-cancer gene-directed enzyme-prodrug therapy (GDEPT)", ACTA BIOCHIMICA POLONICA, vol. 49, no. 1, 2002, pages 169 - 176, XP008142830 *
See also references of EP2318013A4 *
ZAKHAROV, S. ET AL.: "Catalytic phosphorylation of polyfluoroalkanols. Communication 5. Catalytic phosphorylation of a-polyfluoroalkylbenzyl alcohols with phosphoryl chloride", BULLETIN OF THE ACADEMY OF SCIENCES OF THE USSR, vol. 25, no. 8, 1976, pages 1727 - 1731, XP008142866 *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8664201B2 (en) 2008-07-31 2014-03-04 Ziopharm Oncology, Inc. Synthesis and formulations of salts of isophosphoramide mustard and analogs thereof
US9145431B2 (en) 2008-07-31 2015-09-29 Ziopharm Oncology, Inc. Synthesis and formulations of salts of isophosphoramide mustard and analogs thereof
US9254298B2 (en) 2008-07-31 2016-02-09 Ziopharm Oncology, Inc. Synthesis and formulations of salts of isophosphoramide mustard and analogs thereof
WO2013116281A1 (fr) * 2012-01-31 2013-08-08 Ziopharm Oncology, Inc. Polythérapie à base de moutarde isophosphoramide, d'analogues, ou de sels de celle-ci

Also Published As

Publication number Publication date
TWI454266B (zh) 2014-10-01
BRPI0916739A2 (pt) 2015-11-03
US20140378704A1 (en) 2014-12-25
NZ603801A (en) 2014-01-31
US20110212921A1 (en) 2011-09-01
IL210921A0 (en) 2011-04-28
NZ601139A (en) 2014-02-28
NZ590995A (en) 2012-12-21
US20150328238A1 (en) 2015-11-19
EP2318013A1 (fr) 2011-05-11
US8664201B2 (en) 2014-03-04
SG10201600595PA (en) 2016-02-26
WO2010014841A8 (fr) 2011-02-17
CN102137674A (zh) 2011-07-27
IL210921A (en) 2016-04-21
EP2318013A4 (fr) 2013-07-24
SG183657A1 (en) 2012-09-27
EA201170277A1 (ru) 2011-08-30
JP5769831B2 (ja) 2015-08-26
US20160215005A1 (en) 2016-07-28
ZA201100878B (en) 2011-10-26
KR20110038696A (ko) 2011-04-14
US9254298B2 (en) 2016-02-09
AU2009276512B2 (en) 2014-12-18
CN104490900A (zh) 2015-04-08
AU2009276512A1 (en) 2010-02-04
JP2011529907A (ja) 2011-12-15
JP2014114304A (ja) 2014-06-26
MX2011001122A (es) 2011-03-29
JP5711660B2 (ja) 2015-05-07
US9145431B2 (en) 2015-09-29
EA022655B1 (ru) 2016-02-29
CA2732290A1 (fr) 2010-02-04
TW201004631A (en) 2010-02-01

Similar Documents

Publication Publication Date Title
JP5769831B2 (ja) イソホスホルアミドマスタードおよびその類似体の合成および製剤
KR100858464B1 (ko) 콤브레타스타틴 ａ-4 인산염 프로드럭 모노- 및 디-유기아민 염, 모노- 및 디-아미노산 염, 그리고 모노- 및디-아미노산 에스테르 염
AU2005299385B2 (en) Salts of isophosphoramide mustard and analogs thereof as anti-tumor agents
CZ200331A3 (cs) Deriváty kolchinolu jako inhibitory angiogeneze, způsob jejich přípravy a farmaceutická kompozice, která je obsahuje
DK2581367T3 (en) Salts of isophosphoramid-mustard and analogs thereof
US11434198B2 (en) Compounds and methods for the treatment of neurodegenerative diseases
JP2009536188A (ja) 抗ウイルス性ピリミジンヌクレオシド誘導体
DE102015201148B4 (de) Verwendung von Phenylphosphaten und deren Prodrugs als Arzneimittel in der Krebstherapie
WO2016116603A1 (fr) Nouveaux phénylphosphates et leur utilisation comme médicaments
AU2011221388B2 (en) Salts of isophosphoramide mustard and analogs thereof as anti-tumor agents
WO2023191648A1 (fr) Promédicaments d'opicapone

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 200980133758.X

Country of ref document: CN

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 09803607

Country of ref document: EP

Kind code of ref document: A1

WWE Wipo information: entry into national phase

Ref document number: 2009276512

Country of ref document: AU

ENP Entry into the national phase

Ref document number: 2732290

Country of ref document: CA

Ref document number: 2011521338

Country of ref document: JP

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: MX/A/2011/001122

Country of ref document: MX

NENP Non-entry into the national phase

Ref country code: DE

WWE Wipo information: entry into national phase

Ref document number: 590995

Country of ref document: NZ

WWE Wipo information: entry into national phase

Ref document number: 640/KOLNP/2011

Country of ref document: IN

ENP Entry into the national phase

Ref document number: 2009276512

Country of ref document: AU

Date of ref document: 20090730

Kind code of ref document: A

ENP Entry into the national phase

Ref document number: 20117004208

Country of ref document: KR

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 201170277

Country of ref document: EA

REEP Request for entry into the european phase

Ref document number: 2009803607

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 2009803607

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 13056628

Country of ref document: US

ENP Entry into the national phase

Ref document number: PI0916739

Country of ref document: BR

Kind code of ref document: A2

Effective date: 20110131